O laboratório farmacêutico suíço Roche recebeu autorização da Food and Drug Administration (FDA, a Agência Americana de Alimentos e Medicamentos) para testar um método de diagnóstico da zika.
Apesar de ainda não estar homologado, a FDA aprovou o teste, chamado LightMix Zika, com o argumento de que esta é uma situação de emergência, informou a Roche em um comunicado.
“O LightMix Zika é um teste molecular que permite aos profissionais de saúde detectar rapidamente o vírus” disse Uwe Oberlaender, diretora da Roche Molecular Diagnostics.
O vírus da Zika é considerado responsável pelo aumento de casos demicrocefalia, uma má-formação dos recém-nascidos grave e irreversível, sobretudo na América Latina, e também se acredita que provoca doenças neurológicas em adultos como a síndrome de Guillain-Barré.
O mosquito Aedes aegypti é considerado o principal vetor da transmissão do vírus.
Roche, líder mundial da oncologia, é um dos grandes laboratórios do mundo a desenvolver testes de diagnóstico da zika.
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